• Decrease font size
  • Return font size to normal
  • Increase font size
U.S. Department of Health and Human Services

Manufacturer and User Facility Device Experience (MAUDE)

  • Print
  • Share
  • E-mail
-
Super Search Devices@FDA
510(k) | DeNovo | Registration & Listing | Adverse Events | Recalls | PMA | HDE | Classification | Standards
CFR Title 21 | Radiation-Emitting Products | X-Ray Assembler | Medsun Reports | CLIA | TPLC
 

 
 < 
 1 
 2 
 3 
 
 
21 records meeting your search criteria returned- Product Code: MOZ Patient Problem: Hemorrhage/Bleeding Report Date From: 01/1/2009

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
BIO-TECHNOLOGY GENERAL (ISRAEL) LTD EUFLEXXA 07/13/2017
BIO-TECHNOLOGY GENERAL (ISRAEL) LTD EUFLEXXA 06/08/2017
BIO-TECHNOLOGY GENERAL / FERRING PHARMAC EUFLEXXA 1% SODIUM HYALURONATE 05/26/2017
Unknown Manufacturer ORTHOVISC INJ 15MG/ML 04/21/2017
BIO-TECHNOLOGY GENERAL (ISRAEL) LTD EUFLEXXA 02/23/2017
GENZYME BIOSURGERY (RIDGEFIELD) HYLAN G-F 20 12/23/2016
SEIKAGAKU CORPORATION GEL-ONE 01/19/2016
GENZYME BIOSURGERY (RIDGEFIELD) SYNVISC ONE (SYNVISC ONE) 05/05/2015
GENZYME BIOSURGERY (RIDGEFIELD) SYNVISC ONE 10/21/2014
GENYME BIOSURGERY (RIDGEFIELD) SYNVISC (SYNVISC) 04/09/2014
-
-